chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1093100419310042GC22GENIChomozygous51322558
1093104629310463TC25GENIChomozygous51322559
1093105349310535TC23GENICpossibly homozygous51322560
1093117969311797CA23GENIChomozygous51322561
1093122279312228CA35GENIChomozygous51322562
1093123069312307AG24GENIChomozygous51322563
1093125719312572TA15GENIChomozygous51322564
1093140929314093CT14GENIChomozygous51322565
1093144129314413CT17GENIChomozygous51322566
1093158309315831CCCATGAG27GENIChomozygous51322567
1093161879316188AG26GENIChomozygous51322568
1093175179317518CA22GENIChomozygous51322569
1093176439317644TC20GENIChomozygous51322570
1093179379317938AG33GENIChomozygous51322571
1093182199318220AT34GENIChomozygous51322572
1093187319318732AC29GENIChomozygous51322573
1093188179318818AG20GENIChomozygous51322574
1093192089319209TC30GENIChomozygous51322575
1093194669319467AAG29GENIChomozygous51322576
1093198989319899TC16GENIChomozygous51322577
1093199399319940CG17GENIChomozygous51322578